KLM Laboratories Pvt. Ltd., a leading pharmaceutical company specializing in dermatology, pediatric care, and cosmeceuticals, is hosting a walk-in interview for multiple roles at its state-of-the-art manufacturing unit near Vadodara, Gujarat.
Established in 2010, KLM is EU-GMP and WHO-GMP certified, with a global presence in 10+ countries and a focus on semi-solid and oral dosage forms. Join our team to drive innovative healthcare solutions!
About KLM Laboratories Pvt. Ltd.
Headquartered in Mumbai with a 100,000+ sq. ft. manufacturing facility in Vadodara, KLM Laboratories is renowned for its high-quality topical and oral formulations, including immunomodulators, corticosteroids, and anti-fungal solutions.
Rated 4.0/5 on AmbitionBox for job security (4.0/5), employees appreciate skill development (3.8/5) but note challenges with work-life balance (3.6/5) due to rotational shifts and project deadlines.
With over 1,000 professionals and a revenue of ₹100–500 crore, KLM is a top prescriber of Itraconazole in India and serves regulated markets like the EU and ROW (Rest of World).
Open Positions at Vadodara Facility
KLM is hiring for Quality Control (QC), Quality Assurance (QA), Production, Engineering, Packaging & Development, Regulatory Affairs, Research & Development (R&D), and Analytical Development Lab (ADL) roles with 2–12 years of experience. Below are the details.
Quality Control (QC) – Officer / Sr. Officer / Executive
- Qualification: B.Sc / M.Sc / B.Pharm / M.Pharm
- Experience: 2–8 years
- Roles:
- Instrument Analysis: Perform testing using HPLC, GC, UV, FTIR, and dissolution testers
- Reviewer: Review analytical data, reports, and ensure GLP compliance
- Responsibilities:
- Conduct raw material, in-process, and finished product analysis for semi-solid/oral dosage forms
- Validate analytical methods and prepare reports for regulatory audits
- Ensure compliance with USFDA, EU-GMP, and ICH guidelines
- Required Skills:
- Proficiency in HPLC, GC, and analytical techniques
- Knowledge of GLP, GMP, and regulatory audits
- Strong documentation and data review skills
- Vacancies: Multiple
Quality Assurance (QA) – Officer / Sr. Officer / Executive
- Qualification: M.Sc / B.Pharm / M.Pharm
- Experience: 2–8 years
- Responsibilities:
- Manage QMS activities (CAPA, deviations, change control)
- Perform IPQA, line clearance, and BMR/BPR reviews
- Conduct validation activities and support regulatory audits
- Required Skills:
- Expertise in QMS, IPQA, and validation protocols
- Familiarity with USFDA, EU-GMP, and WHO-GMP standards
- Strong analytical and documentation skills
- Vacancies: Multiple
Production – Officer / Sr. Officer / Assistant Manager
- Qualification: M.Sc / B.Pharm / M.Pharm
- Experience: 2–12 years
- Responsibilities:
- Oversee manufacturing of semi-solid products (creams, ointments, gels)
- Manage batch execution, process optimization, and GMP compliance
- Coordinate with QA/QC for in-process checks
- Required Skills:
- Experience in semi-solid formulation manufacturing
- Knowledge of GMP and regulatory audits
- Leadership and process optimization skills
- Vacancies: Multiple
Production – Operator
- Qualification: ITI / Diploma
- Experience: 2–5 years
- Responsibilities:
- Operate manufacturing and filling equipment for semi-solid and liquid products
- Perform cleaning, setup, and documentation per SOPs
- Ensure safety and GMP compliance
- Required Skills:
- Hands-on experience with semi-solid/liquid filling equipment
- Basic knowledge of GMP and safety protocols
- Attention to detail
- Vacancies: Multiple
Engineering – Maintenance & Project Engineer
- Qualification: B.E / B.Tech (Mechanical/Electrical)
- Experience: 6–8 years
- Responsibilities:
- Maintain and troubleshoot plant utilities (HVAC, water systems, boilers)
- Execute engineering projects and ensure equipment uptime
- Support validation and regulatory audits
- Required Skills:
- Expertise in pharma plant maintenance and utilities
- Knowledge of GMP and project execution
- Troubleshooting and coordination skills
- Vacancies: Limited
Packaging & Development – Assistant Manager
- Qualification: Any Graduate
- Experience: 8–12 years
- Responsibilities:
- Develop primary and secondary packaging for semi-solid/oral dosage forms
- Optimize packaging designs for stability and compliance
- Coordinate with vendors and regulatory teams
- Required Skills:
- Experience in pharma packaging development
- Knowledge of packaging materials and regulatory requirements
- Vendor management and project skills
- Vacancies: 1–2
Regulatory Affairs – Executive / Sr. Executive
- Qualification: B.Pharm / M.Pharm
- Experience: 6–10 years
- Responsibilities:
- Prepare and review dossiers (ACTD/CTD) for ROW markets
- Ensure compliance with regional regulatory guidelines
- Support query responses and regulatory audits
- Required Skills:
- Expertise in dossier preparation for ROW markets
- Knowledge of ACTD/CTD formats and regulatory submissions
- Strong documentation and analytical skills
- Vacancies: Multiple
Research & Development (R&D) – Scientist (Various Levels)
- Qualification: M.Pharm / PhD
- Experience: 2–5 years
- Responsibilities:
- Develop semi-solid and oral dosage formulations
- Conduct pre-formulation studies and scale-up activities
- Ensure formulations meet regulatory and commercial requirements
- Required Skills:
- Experience in semi-solid/oral dosage form development
- Knowledge of formulation optimization and scale-up
- Familiarity with USFDA/PIC/S guidelines
- Vacancies: Multiple
Analytical Development Lab (ADL) – Scientist (Various Levels)
- Qualification: M.Sc / M.Pharm
- Experience: 2–5 years
- Responsibilities:
- Develop and validate analytical methods for semi-solid/oral dosage forms
- Perform stability studies and impurity profiling
- Prepare analytical reports for regulatory submissions
- Required Skills:
- Proficiency in method development/validation (HPLC, GC)
- Knowledge of GLP, GMP, and ICH guidelines
- Strong analytical and documentation skills
- Vacancies: Multiple
Walk-In Interview Details
- Date: 22nd June 2025 (Sunday)
- Time: 10:00 AM – 3:00 PM
- Venue: 261, GIDC Makarpura, Bharti House, Bank of Baroda Lane, Vadodara, Gujarat – 390010
- Contact: +91 92278 97864
- Email: career@klmlab.com
- Website: www.klmlab.com
Documents to Bring
- Updated resume with passport-sized photograph
- CTC breakup (current salary details)
- Copies of educational certificates (B.Sc/M.Sc/B.Pharm/M.Pharm/ITI/Diploma/B.E/PhD)
- Aadhaar Card and PAN Card
- Last 3 months’ payslips and increment letter
- Experience certificates or relieving letters
How to Apply
Attend the walk-in interview at the specified venue in Vadodara with the required documents. If unable to attend, email your resume to career@klmlab.com with the subject “Application for [Position Name] – Vadodara – June 2025.”
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Only candidates with relevant pharmaceutical experience (2–12 years) are eligible. Immediate joiners are preferred.
Why Join KLM Laboratories?
KLM Laboratories offers a platform to work in a USFDA and PIC/S-compliant facility with a focus on dermatology and pediatric formulations. Employees benefit from:
- Skill Development: Exposure to advanced semi-solid/oral dosage technologies (3.8/5)
- Job Security: Strong stability in a growing company (4.0/5)
- Global Reach: Opportunities in ROW markets and regulated regions
Benefits: Mediclaim, PF, and festival celebrations (e.g., Holi, cricket leagues) However, rotational shifts and project timelines may impact work-life balance (3.6/5), and some reviews note slow career progression.
Why Vadodara?
KLM’s Vadodara facility in GIDC Makarpura is in a thriving pharmaceutical hub, offering career stability. The location is accessible but may require commuting due to traffic. Ongoing construction of Unit 3 (40,000 sq. ft. warehouse, 30,000 sq. ft. production shed) signals growth opportunities.
Important Notes
- Eligibility: Only candidates with 2–12 years of relevant pharma experience (semi-solid/oral dosage preferred). Male candidates preferred for Production/Engineering roles due to rotational shifts.
- Rotational Shifts: Mandatory for Production and Operator roles.
- Disclaimer: KLM Laboratories does not charge fees for job applications. Use only official contact +91 92278 97864 or career@klmlab.com. Beware of fraudulent offers.
- Note: Candidates interviewed in the last 6 months need not reapply. Expect a fast-paced environment with technical growth but potential shift-related challenges.
Don’t miss this opportunity to join KLM Laboratories Pvt. Ltd.! Attend our walk-in interview on 22nd June 2025 in Vadodara and contribute to innovative healthcare solutions!
